Risperidone and Olanzapine for the Schizophrenic Patients With Neuroleptic-Induced Acute Dystonia or Parkinsonism

Phase 4

Completed

• Conditions: Schizophrenia; Extrapyramidal Syndrome

• Registration Number: NCT00331825
• Lead Sponsor: Taoyuan Psychiatric Center, Ministry of Health and Welfare, Executive Yuan, R.O.C. Taiwan

Brief Summary

We initiate a study with research grant from department of health and Taoyuan mental hospital and choose risperidone and olanzapine as study medications. We compare the incidence of using anticholinergic drugs in schizophrenic patients of Han ethnics with neuroleptic-induced acute dystonia or parkinsonism to test the hypothesis that these two medications have different EPS incidence in EPS intolerant population.

Detailed Description

Objective: First generation antipsychotics frequently induced extrapyramidal side effects (EPS). Second generation antipsychotics were the choices for EPS intolerant schizophrenic patients. But which one of second generation antipsychotic was the better choice did not have definitive results. We compared risperidone and olanzapine in schizophrenic patients with acute dystonia or parkinsonism side effects and observed the incidence of needing concomitant anticholinergic drugs. We also collected the data of average dose of risperidone and olanzapine to help the dosing strategy guidelines for EPS intolerant schizophrenic patients.

Method: This randomized, rater-blind, parallel group, flexible dose study enrolled patients from Taoyuan Mental Hospital from July 2000 to July 2003. Schizophrenia (DSM-IV) patients who met the research criteria of neuroleptic-induced acute dystonia or parkinsonism research criteria of DSM-IV and greater than moderate severity (\>4) of global impression of extrapyramidal syndrome rating scale (ESRS). 70 patients were random assignment to risperidone or olanzapine for 8 weeks. The primary outcome was to compare the incidence of concomitant anticholinergic drugs.

Study Timeline

• Status Verified: 2000-02
• Study Start: 2000-07
• Study Completion: 2003-07
• Study First Submitted: 2006-05-30
• Study First Submitted QC: 2006-05-30
• Last Update Submitted: 2006-05-30
• Study First Posted: 2006-05-31
• Last Update Posted: 2006-05-31

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

• Age of 18-65 y/o;
• Female patients did not have pregnancy plans and must agree to use reliable pregnancy prevention methods if during childbearing age;
• Meet schizophrenia criteria of DSM-IV;
• Fulfill DSM-IV neuroleptic-induced acute dystonia or parkinsonism research criteria, the severity of acute dystonia or parkinsonism was greater than moderate degree (>4) assessed by global impression of Extrapyramidal System Rating Scale (item 43 and 44 of ESRS);
• Patients or legal responsible people agree to join study and sign informed consent

Exclusion Criteria

• Had other axis I diagnosis of DSM-IV;
• Unstable major systemic diseases;
• Had neurological disorder influenced to EPS assessment;
• Substance abuse or dependence other then coffee or tobacco within 6 months before study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Percentage of using concomitant anticholinergic drugs

Secondary Outcome Measures

Name	Time	Method
Scores of Rating Scale (Extrapyramidal System Rating Scale, Brief Psychiatric Rating Scale)

Trial Locations

Locations (1)

Taoyuan Mental Hospital; 🇨🇳 Taoyuan, Taiwan